VRM Vaccines Do Contain Aborted Human Fetal Tissue Vaccine-Resistance-Movement

VRM: Vaccines Do Contain Aborted Human Fetal Tissue
VRM: Vaccines Do Contain Aborted Human Fetal Tissue
31st August 2014 - By Joel Lord
Do vaccines actually contain aborted human fetal tissue?
It seems the majority of pro-vaccine advocates in the community don’t realize, or have
purposefully ignored the fact that the Measles, Mumps, Rubella (MMR) Vaccine contains
aborted fetal tissue. As a Vaccine researcher in the field, I’m coming up against this obstacle
almost every day now.
So let’s set the record straight.
Aborted human fetal (Diploid Cell) tissue is found in the Rubella
portion of the MMR Vaccine formula – Note: ‘the Wistar RA 27/3 strain of live attenuated
rubella virus propagated in WI-38 human diploid lung fibroblasts (Aborted Human Fetal
Tissue).’
Some in the community are still reluctant to admit they’ve been lied to for generations by socalled Government appointed health authorities. There is no safe threshold for any vaccines,
whatsoever.
Measles, Mumps, Rubella Vaccine (series 1st round given at 12-15 months old) – Official
Package Insert:
‘M-M-R II is a sterile lyophilized preparation of (1)
ATTENUVAX* (Measles Virus Vaccine Live), a more attenuated line of measles virus, derived
from Enders’ attenuated Edmonston strain and propagated in chick embryo cell culture; (2)
MUMPSVAX* (Mumps Virus Vaccine Live), the Jeryl Lynn** (B level) strain of mumps virus
propagated in chick embryo cell culture; and (3) MERUVAX* II (Rubella Virus Vaccine Live)
…,‘
In case you missed that reference: ‘the Wistar RA 27/3 strain of live attenuated rubella virus
propagated in WI-38 human diploid lung fibroblasts.’
For those of you still in doubt, meet WI-38.
WI-38 came from lung cells from a female fetus of 3-months (terminated during the 1st
Trimester) gestation: ‘Minced preparations were obtained by cutting the tissue in a Petri dish
containing GM (growth medium) with paired scalpels or a scissors until the size of each piece
approximated l-4 mm3. Fragmented preparations were obtained by tearing apart the tissue with
two pairs of forceps in a Petri dish containing GM until the pieces could no longer conveniently
be grasped and shredded.
The entire contents of the dish were emptied into one or more Pyrex Blake bottles (surface area
100 cmZ), depending on the size of the original starting tissue. The fragmented lungs, for
example, from a three-month-old human fetus were usually placed in four Blake bottles.
Treatment of tissue with trypsin was done, in general, according to the method of Fernandes.‘
Note: ‘Although it cannot be said with certainty that any cell line or cell strain is absolutely free
of contaminating viruses our evidence does not suggest the presence of such viruses…The
question of the presence of latent viruses in any cellular material is one that can probably never
be answered with absolute certainty…‘
Outline of the standard procedure (serial cultivation) & inherent risks (malignant
“contaminating viruses”) involved in procurement of aborted human fetal tissue:
Phase I, or early growth phase, constitutes that period when the cells have been freed from the
intact tissue and are just establishing themselves on glass (primary culture). In general this phase
lasts from 1 to 3 weeks.
Phase II is characterized by rapid cell multiplication and great acid production. During this
phase the diploid strains must be subcultured at least twice a week with split ratios of ‘2 or 3: 1.
This coincides with the formation of confluent sheets.
Phase III or the terminal phase, is characterized by the appearance of debris, reduction of
mitotic activity and a consequently longer period of time for the development of confluent
sheets…However, in interphase cells of Phase III, bizarre nuclear forms (“malignant” cancerous
tissue) and sizes become more frequent and the appearance of these nuclei is reminiscent of
irradiated cultures. Our attempts to reverse Phase III have been uniformly unsuccessful.
It is apparent…that by freezing cells (-70°Celsuis = -94° Farenheit) at each subcultivation or
every few subcultivations one could have cells available at any given time and in almost limitless
numbers.
‘The WI-38 and MRC-5 cell cultures have been used to prepare hundreds of millions of doses of
(following) vaccines – rubella (third component of the MMR series, administered in 2 doses, first
at 12 months old), hepatitis A (administered in 2 doses, first at 12 months old), varicella
(chickenpox, administered in 2 doses, first at 12 months old) and rabies (administered selectively
pending rabies-related emergency).‘ National Network for Immunization Information
According to the Vaccine Industry, material extracted from a human fetus aborted during the
first trimester “does not and cannot form a complete organism and does not constitute a
potential human being”. When a human life is cut short in utero, then reduced to “minced (meat)
preparations of tissue in a Petri dish”…”torn apart with two pairs of forceps until the pieces
could no longer conveniently be grasped and shredded”, labelled as “cell strains (which) do not
and cannot form a complete organism and do not constitute a potential human being”, all in the
name of scientific progress, you know something is definitely wrong with the ethical parameters
supporting Modern Medical research.
The Rubella Vaccine strain (RA 27/3) found in the current MMR Vaccine on the market
originally derived from a stockpile of 27 human fetuses, acquired during the Rubella Epidemic
of 1964 – all contaminated with the Rubella virus (German Measles). “Infected Kidney
‘Fibroblast cells” were extracted from the third specimen, which were then subcultivated, after
which ‘the supernatant fluid (surface liquid after it has been centrifuged) was inoculated directly
into a WI-38 culture (aborted human fetal tissue). Once transferred to WI-38, the RA 27/3
rubella strain was passaged further in the same cell strain.‘
Consequently, the Measles, Mumps, Rubella (MMR) Vaccine is
laced with the contaminated remains of two aborted human fetuses – surface liquid extracted
from a Rubella virus-infected kidney (RA 27/3) combined with intrauterine-infected lung tissue
from a second fetus (WI-38). ‘Thus, rising autistic disorder prevalence is directly related to
vaccines manufactured using human fetal cell lines.‘
Note: Preliminary testing of the Frankenstein concoction was conducted upon “institutionalized
children“, who were force-vaccinated, to observe the results – another crime against the innocent
& defenceless, swept under the carpet by an Industry bent on greed & profits.
Mother & baby-to-be share the same Immune System, during all
three trimesters, while the Fetus is ‘in Utero’, via the Placenta. Those young parents who oppose
vaccinations (ie. the MMR Vaccine) for their family, based primarily on Religious convictions,
demonstrate a wisdom beyond their years, trusting in the body’s innate capacity to overcome
(adapt to) viral infections, such as Measles, through natural exposure in the environment.
They also recognize that it is fundamentally unscientific, let alone unethical, to inject aborted
fetal tissue, laced in the MMR Vaccine, into a child’s bloodstream. Whether you profess science
or faith as your reasoning behind that ultimate conclusion, the bottom line, those with Religious
convictions, who choose to maintain a vaccine-free lifestyle, have seen the light.
Human Diploid Cells (aborted fetal tissue) provide the “Cell culture” in which vaccine formulas
are often grown or nurtured. Current vaccines in circulation which contain aborted fetal tissue
include:
1. Polio vaccine (inactivated/IPV) & Oral Polio (live virus) drops
2. Measles, Mumps, Rubella vaccine/MMR (Rubella component)
3. Diphtheria, Tetanus, Pertussis, Poliomyelitis vaccine (DTaP/TdP)
4. Varicella (Chickenpox) vaccine & Shingles (zoster) vaccine
5. Hepatitis A vaccine
6. Rabies vaccine
‘Some vaccines—rubella, HepA, RAB-HDC, VAR, ZOS, and one form of IPV (the Poliovax
contained in Pentacel)—are grown in cultured human embryo fibroblast cell lines (WI-38 or
MRC-5) because these are the only cells that replicate the viruses in high enough titer for mass
production (the rubella vaccine strain itself was originally isolated from an aborted fetus with
intrauterine infection).‘ Monthly Prescribing Reference (MPR) – Medical Industry Reference
Journal
‘Today, more than 23 vaccines are contaminated by the use of aborted fetal cells. There is no law
that requires that consumers be informed that some vaccines are made using aborted fetal cells
and contain residual aborted fetal DNA. While newer vaccines produced using aborted fetal cells
do inform consumers, in their package inserts, that the vaccines contain contaminating DNA
from the cell used to produce the vaccine, they do not identify the cells as being derived from
electively aborted human fetuses.‘ Dr. Theresa A. Deisher, Ph.D.
‘Not only damaged human cells, but also healthy human cells can take up foreign DNA
spontaneously. Foreign human DNA taken up by human cells will be transported into nuclei and
be integrated into host genome, which will cause phenotype change. Hence, residual human fetal
DNA fragments in vaccine can be one of causes of autism spectrum disorder in children through
vaccination.‘ Spontaneous Integration of Human DNA Fragments into Host – Dr. Genome K.
Koyama, Dr. Theresa. A. Deisher Ph.D.
Study findings: ‘In addition to the ingredients listed on the package insert for Meruvax II®
(Rubella virus vaccine live), we detected significant levels of human ssDNA (142 ± 8 ng/vial) as
well as dsDNA (35 ± 10 ng/vial) fragmented to -215 base pairs in length. The MMR II® package
insert discloses the presence of human fetal residuals nor how much cell substrate dsDNA
(double-stranded DNA) or ssDNA (single-stranded DNA) contaminates each dose.‘ Journal of
Public Health and Epidemiology, 09/2014
Note: ng = nanogram (one billionth of a gram)
‘The children vaccinated with MMRII, Varicella and Hepatitis A vaccines varied from 19 to 35
months of age at the time of vaccination. Autistic disorder birth year change-points (sudden
spike in cases) were identified as 1980.9, 1988.4 and 1996 for the US, 1987 for the UK, 1990.4 for
Western Australia, and 1987.5 for Denmark.
Change points in these countries corresponded to introduction of or increased doses of human
fetal cell line-manufactured vaccines…Further, linear regression revealed that Varicella and
Hepatitis A immunization coverage was significantly correlated to autistic disorder cases.’
Note: ‘Autistic disorder change points years are coincident with introduction of vaccines
manufactured using human fetal cell lines, containing fetal and retroviral contaminants, into
childhood vaccine regimens. Thus, rising autistic disorder prevalence is directly related to
vaccines manufactured using human fetal cell lines.‘
Note: The aforementioned Study verifies that human DNA, the genetic template (blueprint) a
child enters the world equipped with, which determines their capacity to thrive, can, in fact, be
damaged, lessened, rendered defective AFTER birth, post-vaccination; blowing the entire CDC
argument implicating genetics as the primary cause for Autism, completely out of the proverbial
water.
All Standard Immunization-type vaccines in circulation requiring Human Diploid Cells (HDC),
including those discontinued vaccines which utilized HDC since its inception in 1961, have
derived the cell strain culture itself from one exclusive, carefully guarded “batch” or stockpile;
comprising the fetal remains (lung tissue) of a female fetus of 3-months gestation (acquired in
1961/US), and those of a terminated 14-week-old male fetus (acquired in 1966/UK).
Human Fetal Links with Some Vaccines; ‘Human diploid cells are batches of human cells that
are grown in a laboratory. Unlike cancer cells, they have the same number of chromosomes as
normal human cells. Certain diploid cell strains are valuable in vaccine manufacture because
these cells can be used for a very long period of time in the laboratory and are a reliable means
by which many viruses that infect humans can be successfully and easily grown. Vaccines
prepared in human diploid cells have proven to be very safe over the past several decades.
Two different strains of human diploid cell cultures made from fetuses have been used
extensively for vaccine production for decades. One was developed in the United States in 1961
(called WI-38) and the other in the United Kingdom in 1966 (called MRC-5). WI-38 came from
lung cells from a female fetus of 3-months gestation and MRC-5 was developed from lung cells
from a 14-week-old male fetus. Both fetuses were intentionally aborted, but neither was aborted
for the purpose of obtaining diploid cells.123. The fetal tissues that eventually became WI-38 and
the MRC-5 cell cultures were removed from fetuses that were dead. The cellular biologists who
made the cell cultures did not induce the abortions.
These two cell strains have been growing under laboratory conditions for more than 35 years.
The cells are merely the biological system in which the viruses are grown. These cell strains do
not and cannot form a complete organism and do not constitute a potential human being. The
cells reproduce themselves, so there is no need to abort additional fetuses to sustain the culture
supply. Viruses are collected from the diploid cell cultures and then processed further to produce
the vaccine itself.’ National Network For Immunization Information
The introduction of Human Diploid Cells for use in Vaccine Technology followed closely on the
heels of the disastrous Salk & Sabin Polio inoculation campaign; both in the United States (195455) and subsequently in Britain (1957). ‘The introduction of polio immunisation was
accompanied by mass campaigns targeted at all individuals aged less than 40 years.‘
– a time-frame where-in either set of PARENTS from which the Human Diploid Cells specimens
were acquired could obviously have been previously vaccinated with the Salk live Poliomavirus
vaccine.
Therefore, the specimens which comprise the exclusive Human Diploid
Cell culture stockpile may very well have “inadvertently” been co-infected with Simian Virus
SV40 (diseased Rhesus & African Green Monkey tissue culture – strain utilized to nurture
Poliomyelitis, hidden in the germ line DNA of either Fetus – the result of direct SV40
contamination from the Salk Vaccine (live Poliomavirus) co-infecting the DNA of either set of
parents responsible for the baby’s genetic material now in widespread use; subsequently passed
on from mother to Fetus via the Placenta.
An entire generation has since been inoculated with vaccines containing the original Human
Diploid Cell culture set. If, indeed, there was any SV40 cross-contamination embedded in the
lung tissue culture extracted from either Fetus, the primary HDC source in circulation, it is
logical to determine that SV40 cross-contamination has also made its way into those who were
subsequently vaccinated (intramuscularly, subcutaneously or via oral drops) with the same
Human Diploid Cell culture source.
This would certainly explain the recent Controlled Study where-in Simian Virus co-infection was
identified in 67% of post-mortem brains of sufferers of Autism.
New Controlled Study finds poliomavirus infection in post-mortem brains of sufferers of Autism
– 67% infection with Simian Virus (SV40): ‘Vertical viral transmission represents a nongenetic
mechanism of disease compatible with high parent-to-offspring transmission and with low rates
of disease-specific genetic abnormalities. Vertically transmitted viruses should be found more
frequently in the affected tissues of autistic individuals compared to controls. Our initial step was
thus to assess by nested polymerase chain reaction (PCR) and DNA sequence analysis the
presence of cytomegalovirus (CMV), Epstein-Barr virus (EBV), herpes simplex virus type 1
(HSV1), herpes simplex virus type 2 (HSV2), human herpes virus 6 (HHV6), BK virus (BKV),
JC virus (JCV), and simian virus 40 (SV40) in genomic DNA extracted from postmortem
temporocortical tissue (Brodmann areas 41/42) belonging to 15 autistic patients and 13 controls.
BKV, JCV, and SV40 combined are significantly more frequent among autistic patients
compared to controls (67% versus 23%, respectively; P <.05). The majority of positives yielded
archetypal sequences, whereas six patients and two controls unveiled single–base pair changes in
two or more sequenced clones.’ Laboratory of Molecular Psychiatry, Psychiatric
Genetics/Neurogenetics, University Campus Bio-Medico, Rome, Italy
Note: ‘BKV, JCV, and SV40 combined are significantly more frequent among autistic patients
compared to controls (67% versus 23%, respectively; P <.05′
How did Simian Virus get there, you might ask? – Inevitably, the result of vertical transmission
(parent-to-child), viral shedding & inter-generational cross-contamination from Salk & Sabin
Polio inoculations, sugar cube/oral drops versions & the subsequent Inactivated Polio Vaccine
(or IPV) now on the schedule; permanently fixed in (altering) the germ-line DNA of successive
newborns.
‘In recent years more than 60 scientific studies have found SV40 in rare human brain, bone and
lung-related cancers, the same kinds of tumors the virus caused in laboratory animals. Some
scientists believe SV40 may play a role in causing those cancers. One of the biggest mysteries,
however, is why SV40 has been found in tumors removed from people who never received the
contaminated Salk vaccine.‘
There are several possible explanations for this disturbing anomaly:
1. Direct SV40 cross-contamination from the Salk Vaccine (live Poliomavirus) co-infecting the
DNA of either set of parents responsible for the baby’s genetic material now in use; passed on
from mother to child via the Placenta & Colostrum (Endogenous retrovirus).
2. Direct SV40 cross-contamination of the child’s DNA (germ-line mutations) from the Salk
Vaccine (live Poliomavirus), embedded in the Brain white-matter.
3. Indirect SV40 contamination from another vaccine (ie. Inactivated Polio – African Green
Monkey Monkey Kidney “benign” version, Oral Polio drops – African Green Monkey Monkey
Kidney “benign” version), co-infecting the DNA of either set of parents responsible for the
baby’s genetic material now in use; passed on from mother to child via the Placenta &
Colostrum (Endogenous retrovirus).
4. Indirect SV40 contamination from a vaccine derived from contaminated Human Diploid Cell
culture (ie. Inactivated Polio, Oral Polio Drops, Hepatitis A, Measles, MMR – Rubella
component) co-infecting the DNA of either set of parents responsible for the baby’s genetic
material now in use; passed on from mother to child via the Placenta & Colostrum (Endogenous
retrovirus).
5. Indirect SV40 contamination from a vaccine derived from contaminated Human Diploid Cell
culture (ie. Inactivated Polio, Oral Polio Drops, Hepatitis A, Measles, MMR – Rubella
component) co-infecting the child.
6. Indirect SV40 contamination from another Polio type vaccine (ie. Inactivated Polio – African
Green Monkey Monkey Kidney “benign” version, Oral Polio drops – African Green Monkey
Monkey Kidney “benign” version) co-infecting the child.
Note: Given a mother (or father) already has a compromised Immune System and/or preexisting Medical conditions, any such infection/disorder/disease will often factor into the
equation; in terms of co-infecting/altering the DNA genetic blueprint of the offspring/progeny.
‘From 1955 to 1963, the polio vaccine supplied to the United States, Canada, Europe, Asia and
Africa was contaminated with SV40. Furthermore, the possibility of horizontal transmission may
have enlarged this exposure. Many studies have found evidence of SV40 infection. A metaanalysis conducted by Vilchez reviewed molecular, pathological, and clinical data from 1,793
cancer patients. He concluded that there is significant data to support a role for SV40 infection
in human brain cancers, bone cancers, malignant mesothelioma, and non-Hodgkin’s
lymphoma.’ Cleveland College of Medicine
‘Mutations and minority variants, relative to vaccine strains, not known to affect attenuation
were detected in OPV, mumps virus, and varicella-zoster virus. The anticipated detection of
endogenous retroviral sequences from the producer avian and primate cells was confirmed.
Avian leukosis virus (ALV), previously shown to be noninfectious for humans, was present as
RNA in viral particles, while simian retrovirus (SRV) was present as genetically defective DNA.’
Journal of Virology, June 2010 vol. 84 no. 12
Note: ‘simian retrovirus (SRV) was present as genetically defective DNA.’
The multi-billion dollar Vaccine Industry has routinely been utilizing Human Diploid Cells
gathered from sections of a mere two individual Fetuses. But these select babies-to-be didn’t
come out of thin air…they’re not Adam & Eve either. Their individual DNA genetic blueprints,
the unique germ line DNA of either Fetus was determined by each set of parents, whose own
individual DNA genetic blueprint, each unique set of germ-line DNA was previously determined
by their own set of parents.
This has everything to do with history. Endogenous retroviruses – remnants of ancestral
exogenous retroviral infections fixed in the germ-line DNA. And remember, they were both
conceived during one of the darkest chapters in Modern Medical history – that of the disastrous,
misguided Salk & Sabin Polio Vaccine campaign.
There is clear distinction between the verifiable science of the body, and the detritus of
propaganda supporting vaccine theory. There will indeed come a day when vaccination,
vivisection, & irradiation will have gone the way of the dinosaur, replaced by non-invasive,
genuinely holistic techniques; when Allopathic-type medicine, along with all the ancient tools of
its trade, will crumble in the wake of an evolution of consciousness & common sense.
I am now convinced that there is but one path out of the mess created by Western Allopathic
Medicine and all its hazards & mistakes: Just walk away. What I am advocating is making a
clean break, by completely divorcing yourself from all their rhetoric, all the toxic products that
are peddled in the name of mainstream medicine, and returning to that sacred path on which our
ancestors still stand.
The transition to self-sufficiency, in terms of restoring optimal natural health in the body,
requires a genuine paradigm shift in consciousness AWAY from dependency on outside forces, by
reclaiming the inherent instinct for survival and unregulated communal living; where-in we can
relearn the wisdom & knowledge of natural cures (via tinctures, broths, ointments, spices,
essential oils, phytonutrient & antioxidant derived holistic remedies) which our ancestors
coveted and passed on from generation to generation within the community. Their knowledge is
your strength.
Our ancestors are waiting & watching for us to rise up and RECLAIM that which is inherent to
life, a genuine freedom which they once coveted by hook or crook, in far more desperate
circumstances.
So it is now incumbent upon you as an individual to decide the course of your future. Are you
going to serve the profiteers of the Vaccine industry…and join the herd, or continue to stand by
your family?
See: VRM: Measles Report
See: VRM: The Rise of Mutagenic Viruses
VRM: The Autism Report https://vaccineresistancemovement.org/?p=10185
VRM: Worldwide Autism Study Direct link to
study: http://study.vaccineresistancemovement.org/
VRM: The Problem With Vaccines Part 1 https://vaccineresistancemovement.org/?p=488
VRM: Vaccine Clinic – A Concise Compendium To The Problem With
Vaccineshttps://vaccineresistancemovement.org/?p=6278
VRM: The Problem With Vaccines Part 2 – Synergistic Effect of Heavy Metal Toxicity On The
Body https://vaccineresistancemovement.org/?p=6097
VRM: The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural
Immunity https://vaccineresistancemovement.org/?p=6880
VRM: A Concise Compendium To The Problem With Vaccines Part 3 – Synthetic Genomics &
The Death Of Natural Immunity https://vaccineresistancemovement.org/?p=7283
VRM: The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting
Body https://vaccineresistancemovement.org/?p=8787
VRM: The Problem With Vaccines Part 5A – Detoxification & Restoration of the
Body https://vaccineresistancemovement.org/?p=8836
VRM: The Problem With Vaccines Part 5B – Detoxification & Restoration of the
Body https://vaccineresistancemovement.org/?p=8847
VRM: PCV Vaccine Exposed – Breeding Ground For Staphylococcus
Aureus https://vaccineresistancemovement.org/?p=9431
VRM: Pandemic Preparedness & The Dark Agenda
Ahead https://vaccineresistancemovement.org/?p=9460
VRM: Polio – United Nations & The Great Cull https://vaccineresistancemovement.org/?p=4916
VRM: The Re-emergence of Polio in The Third World (compliments of the World Health
Organization & Bill Gates) https://vaccineresistancemovement.org/?p=10091
VRM: Weaponized Polio & The African Green Monkey
Conundrum https://vaccineresistancemovement.org/?p=10727
VRM: Mandatory Vaccinations – How They Will Be Implemente
d https://vaccineresistancemovement.org/?p=11806
VRM: The Confidential Case-files of GlaxoSmithKline – Cover-up, Deferral & Denial of
Responsibility for Vaccine-related Premature Deaths https://vaccineresistancemovement.org/?
p=12242
VRM: Primary Reasons Not To Get The Flu Shot https://vaccineresistancemovement.org/?
p=12642
VRM: The Flu Report https://vaccineresistancemovement.org/?p=9226
VRM: Vaccine Ingredients https://vaccineresistancemovement.org/?p=979
VRM: Safe Alternatives to Vaccines https://vaccineresistancemovement.org/?
p=662%EF%BB%BF
VRM: Family Charts Gradual Decline Of Daughter https://vaccineresistancemovement.org/?
p=3156
VRM: Health Matters Part 1 https://vaccineresistancemovement.org/?p=6719
VRM: Health Matters Part 2 https://vaccineresistancemovement.org/?p=6746%EF%BB%BF
VRM: Alternative Cancer Cures That Work https://vaccineresistancemovement.org/?p=3729
VRM: Pregnancy Tips https://vaccineresistancemovement.org/?p=3270
VRM: H1N1 Shot Reactions – Miscarriages https://vaccineresistancemovement.org/?p=943
VRM: The Vanishing Sperm Count https://vaccineresistancemovement.org/?p=4639
VRM: H1N1 Vaccine Surplus From 2009 Reveals Growing Distrust of Gov’t &
WHO https://vaccineresistancemovement.org/?p=4969
VRM: Flu Death Statistics – WHO & The Big Lie https://vaccineresistancemovement.org/?
p=784
VRM: Vaccine Industry Deception, Propaganda & Media
Collusionhttps://vaccineresistancemovement.org/?p=197
VRM: Birth of Medical & Scientific Dictatorship – Future
Scenarios https://vaccineresistancemovement.org/?p=997
VRM: H1N1 Bio-weaponry Incorporated https://vaccineresistancemovement.org/?p=884
VRM: Aids & The WHO Connection – Criminal Intent https://vaccineresistancemovement.org/?
p=1749
VRM: Morgellons Syndrome & Chemtrails https://vaccineresistancemovement.org/?p=839
VRM: Council On Foreign Relations 10/16/09- Major Influence on Government Vaccine
Policyhttps://vaccineresistancemovement.org/?p=1880
VRM: Closed Door CDC Meeting Reveals Industry Cover-up Of Heavy Metal Toxicity In
Vaccines https://vaccineresistancemovement.org/?p=5935
VRM: The Rockefeller Foundation Drafts A Post-Pandemic
Scenario https://vaccineresistancemovement.org/?p=5102
VRM: World Health Organization & Vaccine Manufacturers Implicated In Massive H1N1
Financial Scam Involving Kickbacks & Cover-ups https://vaccineresistancemovement.org/?
p=4610
VRM Live – 01/28/11: Vaccine Resistance Movement founder Joel Lord discusses Synthetic
Genomics, cloned cell vaccine technology & the death of natural immunity, gutter journalism &
Dr. Wakefield’s imminent vindication with ‘Truth to Power’ host Paul
Mabelis. http://www.blogtalkradio.com/empradio/2011/01/28/truth-to-power-thursday
VRM Live – 11/04/10: Vaccine Resistance Movement founder Joel Lord lays out the whole
vaccine process with Paul Mabelis; including heavy metal toxicity, synergy, pregnancy issues &
the basic principles of natural health at risk. http://www.blogtalkradio.com/show.aspx?
userurl=empradio&year=2010&month=11&day=05&url=truth-to-power-thursday
VRM Live – 09/24/10: Vaccine Resistance Movement Founder Joel Lord & activist/radio host
Jesse Calhoun lay it all out tonite. Topics include the VRM Worldwide Autism
Study, Scientific/Medical dictatorship, Natural Rights & Vaccine Industry fraud exposed. Special
thanks to host Paul Mabelis. http://www.blogtalkradio.com/empradio/2010/09/24/truth-to-powerthursday
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VRM: Vaccines Do Contain Aborted Human Fetal Tissue – Heatlh news and
more on December 20, 2016
[…] VRM: Vaccines Do Contain Aborted Human Fetal Tissue Do vaccines actually contain
aborted human fetal tissue? It seems the majority of pro-vaccine advocates in the community
don’t realize, or have purposefully ignored the fact that the Measles, Mumps, Rubella (MMR)
Vaccine contains aborted fetal tissue. As a Vaccine researcher in the field, I’m coming up against
this obstacle almost every day now. So let’s set the record straight. baby_fetusAborted human
fetal (Diploid Cell) tissue is found in the Rubella portion of the MMR Vaccine formula – Note:
‘the Wistar RA 27/3 strain of live attenuated rubella virus propagated in WI-38 human diploid
lung fibroblasts (Aborted Human Fetal Tissue).’ Some in the community are still reluctant to
admit they’ve been lied to for generations by so-called Government appointed health authorities.
There is no safe threshold for any vaccines, whatsoever. Measles, Mumps, Rubella Vaccine
(series 1st round given at 12-15 months old) – Official Package Insert: mmr203‘M-M-R II is a
sterile lyophilized preparation of (1) ATTENUVAX* (Measles Virus Vaccine Live), a more
attenuated line of measles virus, derived from Enders’ attenuated Edmonston strain and
propagated in chick embryo cell culture; (2) MUMPSVAX* (Mumps Virus Vaccine Live), the
Jeryl Lynn** (B level) strain of mumps virus propagated in chick embryo cell culture; and (3)
MERUVAX* II (Rubella Virus Vaccine Live)…,‘ In case you missed that reference: ‘the Wistar
RA 27/3 strain of live attenuated rubella virus propagated in WI-38 human diploid lung
fibroblasts.’ For those of you still in doubt, meet WI-38. WI-38 came from lung cells from a
female fetus of 3-months (terminated during the 1st Trimester) gestation: ‘Minced preparations
were obtained by cutting the tissue in a Petri dish containing GM (growth medium) with paired
scalpels or a scissors until the size of each piece approximated l-4 mm3. Fragmented
preparations were obtained by tearing apart the tissue with two pairs of forceps in a Petri dish
containing GM until the pieces could no longer conveniently be grasped and shredded. […]